A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050694



Internal ID19139913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4248610..4264606hg38UCSC Ensembl
Innerchr10:4290802..4306798hg19UCSC Ensembl
Innerchr10:4280802..4296798hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3815997
hg1915997
hg1815997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3489128, nssv3501876
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050694
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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